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Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.156344529C= , CM000667.2:g.156344529C=
GRCh38
NC_000005.9:g.155771539C= , CM000667.1:g.155771539C=
GRCh37
NC_000005.8:g.155704117C=
NCBI36
NG_008693.2:g.479186C= , LRG_205:g.479186C=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000337851.9:c.44C=
MANE Select
ENSP00000338343.4:p.Pro15=
ENST00000337851.8:c.44C=
ENSP00000338343.4:p.Pro15=
ENST00000435422.7:c.41C=
ENSP00000403003.2:p.Pro14=
ENST00000517913.5:c.44C=
ENSP00000429378.1:p.Pro15=
ENST00000524347.2:c.44C=
ENSP00000430794.1:p.Pro15=
NM_000337.5:c.44C= , LRG_205t1:c.44C=
NP_000328.2:p.Pro15=
NM_001128209.1:c.41C=
NP_001121681.1:p.Pro14=
NM_172244.2:c.44C=
NP_758447.1:p.Pro15=
XM_005265966.3:c.44C=
XP_005266023.1:p.Pro15=
XM_005265967.1:c.44C=
XP_005266024.1:p.Pro15=
XM_006714911.2:c.44C=
XP_006714974.1:p.Pro15=
XM_011534621.1:c.41C=
XP_011532923.1:p.Pro14=
XR_941123.1:n.254+2924G=
XM_005265966.5:c.44C=
XP_005266023.1:p.Pro15=
XM_005265967.2:c.44C=
XP_005266024.1:p.Pro15=
XM_011534621.2:c.41C=
XP_011532923.1:p.Pro14=
XM_017009723.2:c.44C=
XP_016865212.1:p.Pro15=
XM_017009724.1:c.44C=
XP_016865213.1:p.Pro15=
NM_001128209.2:c.41C=
NP_001121681.1:p.Pro14=
NM_172244.3:c.44C=
NP_758447.1:p.Pro15=
NM_000337.6:c.44C=
MANE Select
NP_000328.2:p.Pro15=